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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395344Erstellt: 23. Oktober 2026

Tetrahydrofuran → N-(4-Chloro-2-cyanophenyl)-2-(5-morpholin-4ylbenzimidazol-2-yl)acetamide

https://huagongshe.com/de/reaction/395344

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
Edukt2-Amino-5-chlorobenzonitrileHCID 80019—
EduktLithium HexamethyldisilazideHCID 2733832—
EduktEthyl 2-[5-(2-morpholin-4-ylethoxy)benzimidazol-2-yl]acetateHCID 12988786—
ProduktN-(4-Chloro-2-cyanophenyl)-2-(5-morpholin-4ylbenzimidazol-2-yl)acetamideHCID 22664809—

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

LiHMDS (2.5 eq) was added to ethyl 2-[5-(2-morpholin-4-ylethoxy)benzimidazol-2-yl]acetate (1.0 eq) in THF at −78° C. After 1 hour, 2-amino-5-chlorobenzenecarbonitrile (0.82 eq) in THF was added. The reaction was allowed to warm to 23° C. and stirred overnight. The resulting mixture was quenched with NH4Cl (aqueous saturated solution) and extracted with EtOAc. The combined organic layers were washed with H2O and brine, dried over Na2SO4, filtered and concentrated in vacuo to yield a brown solid. The crude material was purified by silica gel chromatography (5:1 EtOAc:hexane) to give the desired product. LC/MS m/z 396.1 (MH+), Rf 1.79 minutes.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605617B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-31fb1ab8829c49f191a7f1634835eb16
Quellennotizuspto-grants-2003_08